SCA Pharmaceuticals recalls hydrocodone injections with potential lack of sterility. Affected products include specific lot numbers and expiration dates. Consumers should check their product details and contact the manufacturer for guidance.
Lack of Assurance of Sterility
SCA Pharmaceuticals is recalling hydrocodone injections that may not be sterile. This could lead to infections if used improperly. The recall affects specific lot numbers and expiration dates.
The product lacks assurance of sterility, meaning it could contain harmful bacteria or other contaminants. This poses a risk of infection when injected into the body, especially in medical settings where sterile conditions are critical.
Individuals who have received the recalled hydrocodone injections for medical use are affected. Patients using these injections for pain management are at risk of infection if the product is not sterile.
Check the product label for the lot number and expiration date. The recalled products have specific lot numbers listed in the recall notice, including expiration dates up to January 29, 2024.
Identify the lot number and expiration date on the product label to determine if it is affected.
The product lacks assurance of sterility, which could lead to infections if used improperly.
Check the product label for the lot number and expiration date. If it matches the recalled products, contact SCA Pharmaceuticals for further instructions.
The recall indicates a potential risk of infection due to lack of sterility, but the official notice does not specify the severity of injury.
We’ve drafted a message you can send SCA Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0405-2024 — SCA Pharmaceuticals SCA Pharmaceuticals Hello, I own a SCA Pharmaceuticals that is covered by recall D-0405-2024 from SCA Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
